Label: EXDEPLOY 5% MINOXIDIL TOPICAL GEL- minoxidil gel
- NDC Code(s): 83767-201-01, 83767-201-02
- Packager: Guangzhou Ruijiu Electronic Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 9, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
-
DO NOT USE
Your amount of hair loss is different than that shown the side of this carton, 5% Minoxidil Gel is not intended for fronta baldness or receding hairline.
Your hair loss is sudden and/or patch.
You do not know the reason for your hair loss.
You are under 18years of age. Do not use on babies and children.
Your scalp is red,inflamed,infected,irritated,or painful.
You use other medicines on the scalp. -
WHEN USING
Do not apply on other parts of the body. Avoid contact with eyes.In case of accidental contact,rinse eyes with a large amount of cool tap water lt takes time to regrow hair.
You may need to use this product 1 times a day for at least 3 months before you see results, The amount of hair regrowth is different for each person.The product will not work for everyone. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Keep the bottle open by turning the cap. Squeeze bottlegently when using. Apply 3-5 drops of minoxidil gel directlyto the scalp in the area to be treated.
Just apply it with the tip of the bottle and spread it out, you don't
even need to massage it in with your hands. lt's very easy to use.
Rotate the cap to reseal the bottle.
Using more often or increasing the amount will not improveresults; consistent use is essential to promote and maintainhair regrowth. - STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EXDEPLOY 5% MINOXIDIL TOPICAL GEL
minoxidil gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83767-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) LACTIC ACID (UNII: 33X04XA5AT) POLYSORBATE 60 (UNII: CAL22UVI4M) WATER (UNII: 059QF0KO0R) BIOTIN (UNII: 6SO6U10H04) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83767-201-01 2 in 1 BOX 03/08/2024 1 60 g in 1 CAN; Type 0: Not a Combination Product 2 NDC:83767-201-02 3 in 1 BOX 03/08/2024 2 60 g in 1 CAN; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 03/08/2024 Labeler - Guangzhou Ruijiu Electronic Technology Co., Ltd. (631973699) Registrant - Guangzhou Ruijiu Electronic Technology Co., Ltd. (631973699) Establishment Name Address ID/FEI Business Operations Guangzhou Ruijiu Electronic Technology Co., Ltd. 631973699 manufacture(83767-201)
